Good Sense 810.003/810AA

Manufacturer
Perrigo Direct, Inc | Nice-Pak Products, LLC
Effective date
2026-04-07
Label type
HUMAN OTC DRUG LABEL
Version
21
Source
full-release
Hydrated at
2026-06-01 01:53:06

Label at a glance#

Product70%
Active ingredientISOPROPYL ALCOHOL
Label structure15 sections

Indications and uses

First aid to help prevent the risk of infection in: minor cuts  scrapes  burns

Dosage and administration

clean the affected area spray a small amount of this product on the affected area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in:

  • minor cuts 
  • scrapes 
  • burns

Warnings

WARNINGS SECTION

For external use only. If taken internally serious gastric disturbances will result.

Flammable

SPL UNCLASSIFIED SECTION

Keep away from fire or flame, heat, spark, electrical

  • do not use as a fuel source. If exposed to a heat source, vapors may ignite, resulting in severe burns, serious injury, or death.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

for deep or puncture wounds, animal bites or serious burns

When using theis product

OTC - WHEN USING SECTION

  • do not get into eyes
  • do not inhale
  • do not apply over large areas of the body
  • do not use longer than 1 week
  • use only as directed

Stop use and ask a doctor

OTC - STOP USE SECTION

if condition persists or gets worse

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical hep or contact a Poison Control Center right away.

Caution

WARNINGS AND PRECAUTIONS SECTION

Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • spray a small amount of this product on the affected area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first

Other information

OTHER SAFETY INFORMATION

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive ingredient

INACTIVE INGREDIENT SECTION

water

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Distributed By: Perrigo Direct, Inc.

Peachtree City, GA 30269

www.PerrigoDirect.com 

GoodSense is a registered trademark of Perrigo Pharma International DAC.

Pat. D675, 101

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 50804-810-45

GoodSense ®

70% Isopropyl Alcohol

  • First Aid Antisetpic
  • For Rubbing and Massaging

WARNING FLAMMABLE 

  • Keep away from heat, spark, electrical, fire or flame
  • DANGER: DO NOT USE AS A FUEL SOURCE.

If exposed to a heat source, vapors may ignite, resulting in severe burns, serious injury, or death.

CAUTION: Do not point at self or others; product will squirt when squeezed.

Use only as directed, in a well-ventilated area; fumes can be harmful.

100% SATISFACTION GUARANTEED

32 FL OZ (1 QT) 946 mL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1014638isopropyl alcohol 70 % Topical SprayPSN21
1014638isopropyl alcohol 0.7 ML/ML Topical SpraySCD21
1014638isopropyl alcohol 70 % Topical SpraySY21

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130079068000970GTIN-13: 0079068000970
EAN-13: 0079068000970
GTIN-12: 079068000970
UPC-A: 079068000970
GTIN storage (14 digits): 00079068000970
mm02.jpg
Data codeData MatrixL0003357BDmm02.jpg
Data codeData MatrixL0003357FDmm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50804-810-0870%3785 mL in 1 BOTTLE, PLASTICLIQUID378521
50804-810-4370%473 mL in 1 BOTTLE, PLASTICLIQUID47321
50804-810-4570%946 mL in 1 BOTTLE, PLASTICLIQUID94621
50804-810-7270%295 mL in 1 BOTTLE, SPRAYLIQUID29521

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50804-810-43ML - Milliliter50804-8105802a501-5a4d-4c49-9e75-628612aba40112022-03-09
50804-810-72ML - Milliliter50804-81047818bc4-6bf0-4ca6-9e85-393da0c70bc312022-09-12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ISOPROPYL ALCOHOLACTIVE INGREDIENTND2M4163021
ISOPROPYL ALCOHOLACTIVE MOIETYND2M4163021
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50804-81050804-810-43, 50804-810-45, 50804-810-72, 50804-810-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
202026-02-19monthly-update2026-06-03 17:56:40

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
70%ISOPROPYL ALCOHOLPerrigo Direct, Incf953a249-07ad-40a1-8aea-b2d419fd3d4d2026-04-07Warnings, Adverse reactionsExact identifier
ndc (package): 50804-810-72
ndc (package): 50804-810-08
ndc (package): 50804-810-45
ndc (package): 50804-810-43
ndc (product): 50804-810
ndc11 (package): 50804081043
ndc11 (package): 50804081072
ndc11 (package): 50804081045
ndc11 (package): 50804081008
spl id: 4ee1ab96-2722-0423-e063-6394a90a69ee
spl set id: f953a249-07ad-40a1-8aea-b2d419fd3d4d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.